These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 8088798

  • 1. Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism.
    Stoffel M, Espinosa R, Powell KL, Philipson LH, Le Beau MM, Bell GI.
    Genomics; 1994 May 01; 21(1):254-6. PubMed ID: 8088798
    [Abstract] [Full Text] [Related]

  • 2. Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms.
    Yamada Y, Stoffel M, Espinosa R, Xiang KS, Seino M, Seino S, Le Beau MM, Bell GI.
    Genomics; 1993 Feb 01; 15(2):449-52. PubMed ID: 8449518
    [Abstract] [Full Text] [Related]

  • 3. The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism.
    Hugnot JP, Pedeutour F, Le Calvez C, Grosgeorge J, Passage E, Fontes M, Lazdunski M.
    Genomics; 1997 Jan 01; 39(1):113-6. PubMed ID: 9027495
    [Abstract] [Full Text] [Related]

  • 4. Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism.
    Jones EM, Menzel S, Espinosa R, Le Beau MM, Bell GI, Takeda J.
    Genomics; 1994 Sep 15; 23(2):490-1. PubMed ID: 7835902
    [Abstract] [Full Text] [Related]

  • 5. Mitochondrial FAD-glycerophosphate dehydrogenase and G-protein-coupled inwardly rectifying K+ channel: No evidence for linkage in maturity-onset diabetes of the young or NIDDM.
    Warren-Perry MG, Stoffel M, Saker PJ, Zhang Y, Brown LJ, MacDonald MJ, Turner RC.
    Diabetes; 1996 May 15; 45(5):639-41. PubMed ID: 8621016
    [Abstract] [Full Text] [Related]

  • 6. Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel.
    Kubo Y, Reuveny E, Slesinger PA, Jan YN, Jan LY.
    Nature; 1993 Aug 26; 364(6440):802-6. PubMed ID: 8355805
    [Abstract] [Full Text] [Related]

  • 7. Partial gene structure and assignment to chromosome 2q37 of the human inwardly rectifying K+ channel (Kir7.1) gene (KCNJ13).
    Derst C, Döring F, Preisig-Müller R, Daut J, Karschin A, Jeck N, Weber S, Engel H, Grzeschik KH.
    Genomics; 1998 Dec 15; 54(3):560-3. PubMed ID: 9878260
    [Abstract] [Full Text] [Related]

  • 8. Assignment of the gene encoding inwardly rectifying potassium channel, subfamily J, member 3 (Kcnj3) to rat chromosome 3q32 by in situ hybridization and radiation hybrid mapping.
    Kreutz R, Zürcher H, Szpirer J, Paul M, Szpirer C.
    Cytogenet Cell Genet; 1999 Dec 15; 87(3-4):269-70. PubMed ID: 10702690
    [No Abstract] [Full Text] [Related]

  • 9. Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map.
    Todd S, Sherman SL, Naylor SL.
    Genomics; 1993 Jun 15; 16(3):612-8. PubMed ID: 8100800
    [Abstract] [Full Text] [Related]

  • 10. Confirmation of the assignment of the gene encoding Kv1.3, a voltage-gated potassium channel (KCNA3) to the proximal short arm of human chromosome 1.
    Folander K, Douglass J, Swanson R.
    Genomics; 1994 Sep 01; 23(1):295-6. PubMed ID: 7829094
    [No Abstract] [Full Text] [Related]

  • 11. Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36.
    Su YR, Klanke CA, Houseal TW, Linn SC, Burk SE, Varvil TS, Otterud BE, Shull GE, Leppert MF, Menon AG.
    Genomics; 1994 Aug 01; 22(3):605-9. PubMed ID: 8001971
    [Abstract] [Full Text] [Related]

  • 12. Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA.
    Yano H, Philipson LH, Kugler JL, Tokuyama Y, Davis EM, Le Beau MM, Nelson DJ, Bell GI, Takeda J.
    Mol Pharmacol; 1994 May 01; 45(5):854-60. PubMed ID: 8190102
    [Abstract] [Full Text] [Related]

  • 13. Isolation and mapping of 45 NotI linking clones to chromosome 22.
    Sanson M, Zhang F, Demczuk S, Delattre O, DeJong P, Aurias A, Thomas G, Rouleau GA.
    Genomics; 1993 Sep 01; 17(3):776-9. PubMed ID: 8244398
    [Abstract] [Full Text] [Related]

  • 14. Assignment of human G-protein-coupled inward rectifier K+ channel homolog GIRK3 gene to chromosome 1q21-q23.
    Lesage F, Fink M, Barhanin J, Lazdunski M, Mattéi MG.
    Genomics; 1995 Oct 10; 29(3):808-9. PubMed ID: 8575783
    [No Abstract] [Full Text] [Related]

  • 15. Characterization and chromosomal localization of the human A2a adenosine receptor gene: ADORA2A.
    Le F, Townsend-Nicholson A, Baker E, Sutherland GR, Schofield PR.
    Biochem Biophys Res Commun; 1996 Jun 14; 223(2):461-7. PubMed ID: 8670304
    [Abstract] [Full Text] [Related]

  • 16. The human interleukin-1 receptor antagonist (IL1RN) gene is located in the chromosome 2q14 region.
    Patterson D, Jones C, Hart I, Bleskan J, Berger R, Geyer D, Eisenberg SP, Smith MF, Arend WP.
    Genomics; 1993 Jan 14; 15(1):173-6. PubMed ID: 8432529
    [Abstract] [Full Text] [Related]

  • 17. Genomic organization and promoter analysis of the human G-protein-coupled K+ channel Kir3.1 (KCNJ3/HGIRK1).
    Schoots O, Voskoglou T, Van Tol HH.
    Genomics; 1997 Feb 01; 39(3):279-88. PubMed ID: 9119365
    [Abstract] [Full Text] [Related]

  • 18. Regional assignment of a human DNA repair gene (XRCC5) to 2q35 by X-ray hybrid mapping.
    Chen DJ, Marrone BL, Nguyen T, Stackhouse M, Zhao Y, Siciliano MJ.
    Genomics; 1994 May 15; 21(2):423-7. PubMed ID: 8088837
    [Abstract] [Full Text] [Related]

  • 19. Human ciliary neurotrophic factor: localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat.
    Lev AA, Rosen DR, Kos C, Clifford E, Landes G, Hauser SL, Brown RH.
    Genomics; 1993 May 15; 16(2):539-41. PubMed ID: 8314594
    [Abstract] [Full Text] [Related]

  • 20. Assignment of the human type I IMP dehydrogenase gene (IMPDH1) to chromosome 7q31.3-q32).
    Gu JJ, Kaiser-Rogers K, Rao K, Mitchell BS.
    Genomics; 1994 Nov 01; 24(1):179-81. PubMed ID: 7896275
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.